Difference between revisions of "Biphenotypic sinonasal sarcoma"
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{{ Infobox diagnosis | {{ Infobox diagnosis | ||
| Name = {{PAGENAME}} | | Name = {{PAGENAME}} | ||
| Image = | | Image = Biphenotypic Sinonasal Sarcoma LDRT 12255.tif | ||
| Width = | | Width = | ||
| Caption = | | Caption = [[Micrograph]] showing a biphenotypic sinonasal sarcoma. [[H&E stain]]. (WC/LESTERTHEINVESTOR) | ||
| Synonyms = low-grade sinonasal sarcoma with neural and myogenic features | | Synonyms = low-grade sinonasal sarcoma with neural and myogenic features | ||
| Micro = bland hypercellular stroma typically without many mitoses, invaginating glandular epithelium | | Micro = bland hypercellular stroma typically without many mitoses, invaginating glandular epithelium | ||
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| Signs = | | Signs = | ||
| Symptoms = | | Symptoms = | ||
| Prevalence = very rare ~ large series 28 | | Prevalence = very rare ~ large series 28 individuals as of 2012 | ||
| Bloodwork = | | Bloodwork = | ||
| Rads = | | Rads = | ||
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*Benign [[nasal polyp]]. | *Benign [[nasal polyp]]. | ||
===Images=== | |||
<gallery> | |||
Image: Biphenotypic Sinonasal Sarcoma LDRT 12255.tif | BSS. (WC) | |||
Image: Biphenotypic Sinonasal Sarcoma LDRT 12256.tif | BSS. (WC) | |||
</gallery> | |||
==IHC== | ==IHC== | ||
Features: | Features: | ||
Revision as of 14:18, 19 November 2018
| Biphenotypic sinonasal sarcoma | |
|---|---|
| Diagnosis in short | |
 Micrograph showing a biphenotypic sinonasal sarcoma. H&E stain. (WC/LESTERTHEINVESTOR) | |
|
| |
| Synonyms | low-grade sinonasal sarcoma with neural and myogenic features |
|
| |
| LM | bland hypercellular stroma typically without many mitoses, invaginating glandular epithelium |
| LM DDx | solitary fibrous tumour, schwannoma, sinonasal-type hemangiopericytoma, benign nasal polyp |
| IHC | S-100 +ve, actin +ve, beta-catenin +ve (nuclear) |
| Molecular | PAX3-MAML3 fusion - t(2;4)(q35;q31.1) |
| Site | head and neck - ethmoid sinus and/or nasal cavity |
|
| |
| Clinical history | female predominant (3:1) |
| Prevalence | very rare ~ large series 28 individuals as of 2012 |
Biphenotypic sinonasal sarcoma, abbreviated SNS,[1] is a rare bland appearing malignant tumour of the head and neck.
It is also known as low-grade sinonasal sarcoma with neural and myogenic features.[2]
General
- Rare - largest series published (as of 2012) 28 patients.[3]
- Female predominant - (female:male = 3:1[3]).
Prognosis:
- No (far away) metastasis or death in a series of 28 patients.[3]
Gross
- Usually ethmoid sinus and/or nasal cavity.[3]
Microscopic
Features:
- Bland hypercellular stroma typically without many mitoses.
- Invaginating glandular epithelium.
Note:
- May have rhabdomyoblastic differentiation - case report.[4]
DDx:
Images
BSS. (WC)
BSS. (WC)
IHC
Features:
- S-100 +ve - strong (28 +ve of 28 cases[3]).
- Actin +ve (27 +ve of 28 cases[3]).
- Beta-catenin - nuclear +ve.[5][2]
Others:[2]
- Desmin -ve.
- AE1/AE3 -ve.
- Vimentin +ve.
Molecular
- PAX3-MAML3 fusion - t(2;4)(q35;q31.1).[1]
See also
References
- ↑ 1.0 1.1 Wang, X.; Bledsoe, KL.; Graham, RP.; Asmann, YW.; Viswanatha, DS.; Lewis, JE.; Lewis, JT.; Chou, MM. et al. (Jul 2014). "Recurrent PAX3-MAML3 fusion in biphenotypic sinonasal sarcoma.". Nat Genet 46 (7): 666-8. doi:10.1038/ng.2989. PMID 24859338.
- ↑ 2.0 2.1 2.2 Powers, KA.; Han, LM.; Chiu, AG.; Aly, FZ. (May 2015). "Low-grade sinonasal sarcoma with neural and myogenic features--diagnostic challenge and pathogenic insight.". Oral Surg Oral Med Oral Pathol Oral Radiol 119 (5): e265-9. doi:10.1016/j.oooo.2014.10.007. PMID 25488011.
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 Lewis, JT.; Oliveira, AM.; Nascimento, AG.; Schembri-Wismayer, D.; Moore, EA.; Olsen, KD.; Garcia, JG.; Lonzo, ML. et al. (Apr 2012). "Low-grade sinonasal sarcoma with neural and myogenic features: a clinicopathologic analysis of 28 cases.". Am J Surg Pathol 36 (4): 517-25. doi:10.1097/PAS.0b013e3182426886. PMID 22301502.
- ↑ Huang, SC.; Ghossein, RA.; Bishop, JA.; Zhang, L.; Chen, TC.; Huang, HY.; Antonescu, CR. (Jan 2016). "Novel PAX3-NCOA1 Fusions in Biphenotypic Sinonasal Sarcoma With Focal Rhabdomyoblastic Differentiation.". Am J Surg Pathol 40 (1): 51-9. doi:10.1097/PAS.0000000000000492. PMID 26371783.
- ↑ http://dx.doi.org/10.1016/j.humpath.2016.04.009